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PARA-CARE

K980718 Class II Traditional
Decision Date
1998-03-27
Sponsor / Applicant
Chattanooga Group, Inc.

Technical Specification

510(k) Submission ID K980718
Product Code IMC
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5110
Decision Date 1998-03-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PARA-CARE received FDA 510(k) clearance under submission number K980718, sponsored by Chattanooga Group, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 1998-03-27.

Classification & Regulation

This clearance is catalogued under FDA product code IMC and 21 CFR 890.5110, within the Physical Medicine review panel as a Class II device.